Robert Sebra

26.7k total citations · 1 hit paper
173 papers, 6.0k citations indexed

About

Robert Sebra is a scholar working on Molecular Biology, Epidemiology and Cancer Research. According to data from OpenAlex, Robert Sebra has authored 173 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Molecular Biology, 34 papers in Epidemiology and 25 papers in Cancer Research. Recurrent topics in Robert Sebra's work include Antibiotic Resistance in Bacteria (18 papers), Genomics and Phylogenetic Studies (17 papers) and Cancer Genomics and Diagnostics (16 papers). Robert Sebra is often cited by papers focused on Antibiotic Resistance in Bacteria (18 papers), Genomics and Phylogenetic Studies (17 papers) and Cancer Genomics and Diagnostics (16 papers). Robert Sebra collaborates with scholars based in United States, United Kingdom and Australia. Robert Sebra's co-authors include Gintaras Deikus, Andrew Kasarskis, Eric E. Schadt, Derrick W. Crook, Nicole Stoesser, Christopher N. Bowman, Kristi S. Anseth, Anna E. Sheppard, Tim Peto and Amy J. Mathers and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert Sebra

162 papers receiving 5.9k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Dietary fructose improves intestinal cell survival and nutrient absorption

2021 194 citations Nancy Francoeur, Robert Sebra et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Robert Sebra	2.9k	957	948	798	601	173	6.0k
Hua Zhu	2.5k 0.9×	572 0.6×	364 0.4×	634 0.8×	354 0.6×	311	7.1k
Philippe Bouvet	6.8k 2.4×	794 0.8×	1.4k 1.5×	943 1.2×	1.2k 1.9×	185	10.1k
Raymond Lo	2.9k 1.0×	421 0.4×	434 0.5×	557 0.7×	440 0.7×	17	4.6k
Stuart J. Cordwell	4.0k 1.4×	625 0.7×	331 0.3×	412 0.5×	544 0.9×	137	6.7k
Xiancai Rao	2.6k 0.9×	864 0.9×	381 0.4×	412 0.5×	1.2k 2.0×	122	5.6k
Ronen Hazan	3.3k 1.1×	363 0.4×	794 0.8×	285 0.4×	425 0.7×	89	6.1k
Roger S. Smith	3.2k 1.1×	262 0.3×	1.1k 1.1×	239 0.3×	294 0.5×	67	5.1k
Karen M. Frank	3.0k 1.1×	171 0.2×	758 0.8×	374 0.5×	559 0.9×	73	4.7k
Hongwei D. Yu	2.7k 1.0×	274 0.3×	588 0.6×	179 0.2×	415 0.7×	72	4.2k

Countries citing papers authored by Robert Sebra

Since Specialization

Citations

This map shows the geographic impact of Robert Sebra's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Robert Sebra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Sebra more than expected).

Fields of papers citing papers by Robert Sebra

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert Sebra. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Robert Sebra. The network helps show where Robert Sebra may publish in the future.

Co-authorship network of co-authors of Robert Sebra

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Sebra. A scholar is included among the top collaborators of Robert Sebra based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Robert Sebra. Robert Sebra is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Filipescu, Dan, Saul Carcamo, Navpreet Tung, et al.. (2023). MacroH2A restricts inflammatory gene expression in melanoma cancer-associated fibroblasts by coordinating chromatin looping. Nature Cell Biology. 25(9). 1332–1345. 16 indexed citations

Tieri, David, Oscar L. Rodriguez, Nancy Francoeur, et al.. (2023). FLAIRR-Seq: A Method for Single-Molecule Resolution of Near Full-Length Antibody H Chain Repertoires. The Journal of Immunology. 210(10). 1607–1619. 15 indexed citations

Rutland, John W., Corey M. Gill, Daniel Ranti, et al.. (2022). Association of mutations in DNA polymerase epsilon with increased CD8+ cell infiltration and prolonged progression-free survival in patients with meningiomas. Neurosurgical FOCUS. 52(2). E7–E7. 5 indexed citations

Downie, Jonathan M., Moeen Riaz, Jing Xie, et al.. (2022). Incident Cancer Risk and Signatures Among Older MUTYH Carriers: Analysis of Population-Based and Genomic Cohorts. Cancer Prevention Research. 15(8). 509–519.

Caligiuri, Stephanie P. B., William M. Howe, Lauren Wills, et al.. (2022). Hedgehog-interacting protein acts in the habenula to regulate nicotine intake. Proceedings of the National Academy of Sciences. 119(46). e2209870119–e2209870119. 5 indexed citations

Siddiq, Mustafa M., Sari S. Hannila, Elena Nikulina, et al.. (2021). Extracellular histones, a new class of inhibitory molecules of CNS axonal regeneration. Brain Communications. 3(4). fcab271–fcab271. 5 indexed citations

Riaz, Moeen, Aamira Huq, Joanne Ryan, et al.. (2021). Effect of APOE and a polygenic risk score on incident dementia and cognitive decline in a healthy older population. Aging Cell. 20(6). e13384–e13384. 22 indexed citations

Lacaze, Paul, Moeen Riaz, Robert Sebra, et al.. (2021). Protective lipid-lowering variants in healthy older individuals without coronary heart disease. Open Heart. 8(2). e001710–e001710. 3 indexed citations

AbuOun, Manal, Hannah Jones, Emma Stubberfield, et al.. (2021). A genomic epidemiological study shows that prevalence of antimicrobial resistance in Enterobacterales is associated with the livestock host, as well as antimicrobial usage. Microbial Genomics. 7(10). 32 indexed citations

10.

Tomlinson, Kira L., Tania Wong Fok Lung, Medini K. Annavajhala, et al.. (2021). Staphylococcus aureus induces an itaconate-dominated immunometabolic response that drives biofilm formation. Nature Communications. 12(1). 1399–1399. 94 indexed citations

11.

Wang, Changjiang, Christian V. Forst, Tsui-Wen Chou, et al.. (2020). Cell-to-Cell Variation in Defective Virus Expression and Effects on Host Responses during Influenza Virus Infection. mBio. 11(1). 38 indexed citations

12.

Lacaze, Paul, Kathlyn J. Ronaldson, Eunice J. Zhang, et al.. (2020). Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. Translational Psychiatry. 10(1). 37–37. 26 indexed citations

13.

Dupper, Amy C., Mitchell J. Sullivan, Brianne Ciferri, et al.. (2019). Blurred Molecular Epidemiological Lines Between the Two Dominant Methicillin-Resistant Staphylococcus aureus Clones. Open Forum Infectious Diseases. 6(9). ofz302–ofz302. 9 indexed citations

14.

Miller, Jason, Sergey Koren, Kari A. Dilley, et al.. (2018). Analysis of the Aedes albopictus C6/36 genome provides insight into cell line utility for viral propagation. GigaScience. 7(3). 1–13. 47 indexed citations

15.

Papa, Luena, Eran Zimran, Mansour Djedaini, et al.. (2018). Ex vivo human HSC expansion requires coordination of cellular reprogramming with mitochondrial remodeling and p53 activation. Blood Advances. 2(20). 2766–2779. 32 indexed citations

16.

Xu, Feng, Narjol González‐Escalona, Kevin P. Drees, et al.. (2017). Parallel Evolution of Two Clades of an Atlantic-Endemic Pathogenic Lineage of Vibrio parahaemolyticus by Independent Acquisition of Related Pathogenicity Islands. Applied and Environmental Microbiology. 83(18). 30 indexed citations

17.

Dillon, Marcus M., Way Sung, Robert Sebra, Michael Lynch, & Vaughn S. Cooper. (2016). Genome-Wide Biases in the Rate and Molecular Spectrum of Spontaneous Mutations in Vibrio cholerae and Vibrio fischeri. Molecular Biology and Evolution. 34(1). 93–109. 62 indexed citations

18.

Drees, Kevin P., Jonathan Palmer, Robert Sebra, et al.. (2016). Use of Multiple Sequencing Technologies To Produce a High-Quality Genome of the Fungus Pseudogymnoascus destructans , the Causative Agent of Bat White-Nose Syndrome. Genome Announcements. 4(3). 21 indexed citations

19.

Beaulaurier, John, Xue‐Song Zhang, Shijia Zhu, et al.. (2015). Single molecule-level detection and long read-based phasing of epigenetic variations in bacterial methylomes. Nature Communications. 6(1). 74 indexed citations

20.

Melters, Daniël P., Keith Bradnam, Hugh A. Young, et al.. (2013). Comparative analysis of tandem repeats from hundreds of species reveals unique insights into centromere evolution. Genome biology. 14(1). R10–R10. 348 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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